GapMind for Amino acid biosynthesis

 

Alignments for a candidate for split_metH_2 in Shewanella loihica PV-4

Align Methionine synthase component, methyltransferase domain (EC:2.1.1.13) (characterized)
to candidate 5208198 Shew_0710 B12-dependent methionine synthase (RefSeq)

Query= reanno::Phaeo:GFF1321
         (338 letters)



>FitnessBrowser__PV4:5208198
          Length = 1240

 Score =  114 bits (286), Expect = 1e-29
 Identities = 105/346 (30%), Positives = 158/346 (45%), Gaps = 45/346 (13%)

Query: 12  KDALLADGATGTNLFNMGLQS----GDAPELWNVD-----------EPKKITALYQGAVD 56
           K+ L+ DGA GT + N  L+     G+  + W  D           +P+ I  +++  + 
Sbjct: 23  KEILILDGAMGTMIQNHKLEEADFRGERFKQWPCDLKGNNDLLVLTQPELIKQIHRDYLL 82

Query: 57  AGSDLFLTNTFGGTAARLKLHDAHRRVRELNVAGAELGR----NVADRSERKIAVAGSVG 112
           AG+D+  TNTF  T   +  ++     RE+N+ GA L R     VA  S R+  VAG +G
Sbjct: 83  AGADIIETNTFNATQVAMADYEMQELSREINLEGARLARTACDEVAAESGRQCYVAGVLG 142

Query: 113 PTG---EIMQPVGELSHAL-----AVEMFHEQAEALKEGGVDVLWLETISAPEEYRAAAE 164
           PT     I   V +  +        VE + E  +AL EGG D++ +ETI      +AA  
Sbjct: 143 PTNRTCSISPDVNDPGYRNIHFDDLVEAYIESTQALIEGGADIIMVETIFDTLNAKAALF 202

Query: 165 AFKL--------ADMPWCGTMSFDTAGRTMMGVTSADMAQLVEEFDPAPLAFGANCGTGA 216
           A +           +   GT++ D +GRT+ G T+      +      PL+ G NC  G 
Sbjct: 203 AIETLFDQLGQRLPVMISGTIT-DASGRTLTGQTTEAFYNSLRHV--KPLSIGLNCALGP 259

Query: 217 SDILRTVLGFAAQGTTRPIISKGNAGIPKYVDGHIHYDGTPTLMGE-YAAMARDCGAKII 275
            + LR  +   ++     + +  NAG+P    G   YD TP  M E     A +    II
Sbjct: 260 QE-LRPYVEELSKIAECYVSAHPNAGLPNEFGG---YDETPEQMAEVIGPWAEEGLLNII 315

Query: 276 GGCCGTMPDHLRAMREALDTRPRGE--QLTLERIVEVLGPFTSDSD 319
           GGCCGT PDH++A+R A+      E   L +   +  L P T D+D
Sbjct: 316 GGCCGTTPDHIKAIRAAVIKHGARELPDLPVACRLSGLEPLTIDAD 361


Lambda     K      H
   0.317    0.134    0.397 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 913
Number of extensions: 57
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 338
Length of database: 1240
Length adjustment: 38
Effective length of query: 300
Effective length of database: 1202
Effective search space:   360600
Effective search space used:   360600
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 54 (25.4 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory